X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4330) 4330
Publication (471) 471
Newsletter (180) 180
Newspaper Article (170) 170
Book Chapter (98) 98
Book / eBook (65) 65
Book Review (65) 65
Magazine Article (38) 38
Web Resource (25) 25
Government Document (18) 18
Conference Proceeding (15) 15
Trade Publication Article (12) 12
Dissertation (11) 11
Reference (7) 7
Data Set (2) 2
Report (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (2306) 2306
animals (1804) 1804
index medicus (1551) 1551
prions (1518) 1518
creutzfeldt-jakob disease (1447) 1447
diagnosis (1036) 1036
creutzfeldt-jakob-disease (1012) 1012
prion protein (1005) 1005
female (979) 979
prion diseases (911) 911
male (869) 869
nervous system diseases (844) 844
scrapie (831) 831
clinical neurology (781) 781
proteins (730) 730
neurosciences (700) 700
prion (696) 696
bse (684) 684
prions - genetics (673) 673
brain - pathology (660) 660
mice (660) 660
cattle (658) 658
middle aged (644) 644
research (644) 644
animal diseases (631) 631
sheep (628) 628
creutzfeldt-jakob syndrome - diagnosis (625) 625
bovine spongiform encephalopathy (618) 618
aged (543) 543
prion diseases - diagnosis (525) 525
brain (502) 502
pathology (464) 464
adult (449) 449
veterinary sciences (425) 425
prions - metabolism (424) 424
protein (413) 413
mutation (407) 407
dementia (384) 384
immunohistochemistry (367) 367
creutzfeldt-jakob syndrome - genetics (363) 363
medicine (360) 360
prion disease (348) 348
creutzfeldt-jakob syndrome - pathology (347) 347
research article (346) 346
brain - metabolism (342) 342
infectious diseases (335) 335
disease (315) 315
transmission (310) 310
biochemistry & molecular biology (306) 306
genetic aspects (305) 305
alzheimers-disease (301) 301
analysis (298) 298
spongiform encephalopathy (295) 295
transmissible spongiform encephalopathy (295) 295
biology (293) 293
mental disorders (289) 289
alzheimer's disease (288) 288
magnetic resonance imaging (283) 283
diagnosis, differential (281) 281
neurology (279) 279
spongiform encephalopathies (279) 279
prion diseases - pathology (276) 276
multidisciplinary sciences (275) 275
cerebrospinal-fluid (272) 272
prion diseases - genetics (271) 271
risk factors (268) 268
neurodegenerative diseases (266) 266
medical research (263) 263
health aspects (262) 262
prp (261) 261
genotype (252) 252
chronic wasting disease (251) 251
protein folding (243) 243
prpsc proteins - metabolism (240) 240
transmissible spongiform encephalopathies (237) 237
prions - analysis (231) 231
prion diseases - metabolism (229) 229
prion proteins (227) 227
neurodegeneration (225) 225
prion diseases - transmission (222) 222
epidemiology (217) 217
immunology (215) 215
physiological aspects (213) 213
creutzfeldt-jakob syndrome - transmission (212) 212
virology (212) 212
pathogenesis (211) 211
aged, 80 and over (210) 210
cjd (210) 210
sensitivity and specificity (210) 210
transgenic mice (209) 209
blotting, western (199) 199
encephalopathy, bovine spongiform - diagnosis (198) 198
variant cjd (195) 195
microbiology (194) 194
science (193) 193
creutzfeldt-jakob syndrome - epidemiology (191) 191
variant (191) 191
disease transmission (190) 190
prions - chemistry (188) 188
natural scrapie (187) 187
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4507) 4507
Japanese (77) 77
Turkish (67) 67
French (65) 65
German (65) 65
Spanish (65) 65
Russian (18) 18
Czech (13) 13
Polish (9) 9
Croatian (8) 8
Portuguese (8) 8
Chinese (6) 6
Danish (5) 5
Dutch (4) 4
Hungarian (4) 4
Korean (4) 4
Slovak (4) 4
Italian (3) 3
Serbian (3) 3
Swedish (3) 3
Norwegian (2) 2
Hebrew (1) 1
Icelandic (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2000, Archives of Virology. Supplementum, ISBN 321183530X, Volume 16., ix, 290
Book
European Journal of Neurology, ISSN 1351-5101, 2012, Volume 19, Issue 9, pp. 1159 - 1179
Click here for the corresponding questions to this CME article. 
treatment | management | review | guideline | dementia | diagnosis | recommendation | Treatment | Guideline | Diagnosis | Management | Review | Recommendation | Dementia | DIFFERENTIAL-DIAGNOSIS | ALZHEIMERS-DISEASE | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | POSITRON-EMISSION-TOMOGRAPHY | VASCULAR COGNITIVE IMPAIRMENT | NORMAL-PRESSURE HYDROCEPHALUS | CREUTZFELDT-JAKOB-DISEASE | LEWY BODIES | PROGRESSIVE SUPRANUCLEAR PALSY | PARKINSONS-DISEASE | Parkinson Disease - therapy | Primary Progressive Nonfluent Aphasia - therapy | Lewy Body Disease - diagnosis | Humans | Dementia - diagnosis | Lewy Body Disease - therapy | Alzheimer Disease - diagnosis | Huntington Disease - therapy | Limbic Encephalitis - therapy | Dementia, Vascular - diagnosis | Frontotemporal Lobar Degeneration - diagnosis | Frontotemporal Lobar Degeneration - therapy | Huntington Disease - diagnosis | Dementia, Vascular - therapy | Limbic Encephalitis - diagnosis | Primary Progressive Nonfluent Aphasia - diagnosis | Prion Diseases - diagnosis | Prion Diseases - therapy | Dementia - therapy | Alzheimer Disease - therapy | Hydrocephalus, Normal Pressure - therapy | Supranuclear Palsy, Progressive - therapy | Parkinson Disease - diagnosis | Supranuclear Palsy, Progressive - diagnosis | Hydrocephalus, Normal Pressure - diagnosis | Care and treatment | Parkinson's disease | Huntington's chorea | Analysis | Practice guidelines (Medicine) | Diagnostic imaging | Alzheimer's disease | Disease | Metabolic disorders | Neuroimaging | Hydrocephalus | Neurodegenerative diseases | EEG | Cognitive ability | Cerebrospinal fluid | Huntington's disease | Blood | Genetic screening | Lewy bodies | Reviews | Dementia disorders | Frontotemporal dementia | Prion protein | Movement disorders | progressive supranuclear palsy | Index Medicus
Journal Article
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 04/2018, Volume 50, pp. 292 - 293
The pre-mortem clinical diagnosis of Creutzfeldt–Jakob disease (CJD) is supported by biomarkers, especially cerebrospinal fluid (CSF) 14-3-3 and total tau... 
14-3-3 | Tau | CJD | CSF | CRITERIA | HUMAN PRION DETECTION | CEREBROSPINAL-FLUID | NEUROSCIENCES | CLINICAL NEUROLOGY | Neurosciences | Biosecurity | Creutzfeldt-Jakob disease | Dementia
Journal Article
Prion, ISSN 1933-6896, 01/2019, Volume 13, Issue 1, pp. 141 - 150
The diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) can only be confirmed by abnormal protease-resistant prion protein accumulation in post-mortem brain... 
Deep learning | 14-3-3 | prion diseases | Creutzfeldt-Jakob disease | Tau | α-synuclein | β-amyloid | CEREBROSPINAL-FLUID BIOMARKER | EEG | BIOCHEMISTRY & MOLECULAR BIOLOGY | alpha-synuclein | beta-amyloid | QUAKING-INDUCED CONVERSION | PHOSPHORYLATED-TAU | CSF | SURVEILLANCE | CJD | 14-3-3-PROTEIN
Journal Article
Annals of Clinical and Translational Neurology, ISSN 2328-9503, 02/2017, Volume 4, Issue 2, pp. 139 - 144
Real‐Time Quaking‐Induced Conversion ( RT ‐Qu IC ) testing of human cerebrospinal fluid ( CSF ) is highly sensitive and specific in discriminating sporadic CJD... 
PRION DETECTION | DISCRIMINATION | NEUROSCIENCES | BOVINE SPONGIFORM ENCEPHALOPATHY | CLINICAL NEUROLOGY
Journal Article